Canonical Allele Identifier: CA1479942163
Gene: ADH1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307816_99307817delinsAC , CM000666.2:g.99307816_99307817delinsAC GRCh38
NC_000004.11:g.100228973_100228974delinsAC , CM000666.1:g.100228973_100228974delinsAC GRCh37
NC_000004.10:g.100447996_100447997delinsAC NCBI36
NG_011435.1:g.18599_18600delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.*23_*24delinsGT MANE Select ENSP00000306606.8:n.*23_*24delinsGT
ENST00000305046.12:c.*23_*24delinsGT ENSP00000306606.8:n.*23_*24delinsGT
ENST00000506651.5:c.*23_*24delinsGT ENSP00000425998.2:n.*23_*24delinsGT
ENST00000515694.4:n.3246_3247delinsGT
ENST00000625860.2:c.*23_*24delinsGT ENSP00000486614.1:n.*23_*24delinsGT
NM_000668.5:c.*23_*24delinsGT NP_000659.2:n.*23_*24delinsGT
NM_001286650.1:c.*23_*24delinsGT NP_001273579.1:n.*23_*24delinsGT
NM_000668.6:c.*23_*24delinsGT MANE Select NP_000659.2:n.*23_*24delinsGT
NM_001286650.2:c.*23_*24delinsGT NP_001273579.1:n.*23_*24delinsGT
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